ProfileGDS1065 / 214033_at
TitleMitochondrial encephalomyopathies associated with mitochondrial DNA mutations
OrganismHomo sapiens


wild type A3243G large deletion normal MELAS PEO GSM24652 GSM24653 GSM24654 GSM24655 GSM24656 GSM24657 GSM24658 GSM24659 GSM24660 GSM24661 GSM24662 GSM24663 GSM24664 GSM24665 GSM24666 59% 64% 69% 58% 68% 74% 63% 59% 65% 66% 60% 61% 55% 70% 65% sort by genotype/variation sort by disease state Gene Expression Profile
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SampleTitleValueRank
GSM24652Normal subject 163.359
GSM24653Normal subject 276.364
GSM24654Normal subject 3123.369
GSM24655A3243G-MELAS subject 143.858
GSM24656A3243G-MELAS subject 294.868
GSM24657A3243G-MELAS subject 319674
GSM24658A3243G-MELAS subject 469.263
GSM24659A3243G-PEO subject 152.759
GSM24660A3243G-PEO subject 273.265
GSM24661A3243G-PEO subject 35966
GSM24662A3243G-PEO subject 456.260
GSM24663mtDNA "Common"-deletion subject 17361
GSM24664mtDNA "Common"-deletion subject 296.155
GSM24665mtDNA "Common"-deletion subject 3159.170
GSM24666mtDNA "Common"-deletion subject 4130.165